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Proceedings of the National Academy of Sciences of the United States of America|August 7, 2024
Fast and scalable ensemble learning method for versatile polygenic risk predictionTony Chen, Haoyu Zhang, Rahul Mazumder, et al.Bioinformatics (Oxford, England)|July 13, 2007
Quantitative quality-assessment techniques to compare fractionation and depletion methods in SELDI-TOF mass spectrometry experimentsJaroslaw Harezlak, Mike Wang, David Christiani, et al.Biorxiv : the Preprint Server for Biology|October 27, 2023
Ensembled best subset selection using summary statistics for polygenic risk predictionTony Chen, Haoyu Zhang, Rahul Mazumder, et al.Pharmacoepidemiology and Drug Safety|December 29, 2020
Measured and accounted-for confounding in pharmacoepidemiologic studies: Some thoughts for practitionersJason Roy, Nandita MitraStatistics in Medicine|September 15, 2005
The effect of provider-level ascertainment bias on profiling nursing homesJason Roy, Vincent MorGenetic Epidemiology|April 18, 2012
Sparse principal component analysis for identifying ancestry-informative markers in genome-wide association studiesSeokho Lee, Michael P Epstein, Richard Duncan, et al.Biostatistics (Oxford, England)|March 7, 2013
Test for interactions between a genetic marker set and environment in generalized linear modelsXinyi Lin, Seunggeun Lee, David C Christiani, et al.Nature Genetics|June 13, 2024
Synthetic surrogates improve power for genome-wide association studies of partially missing phenotypes in population biobanksZachary R McCaw, Jianhui Gao, Xihong Lin, et al.American Journal of Human Genetics|June 18, 2013
General framework for meta-analysis of rare variants in sequencing association studiesSeunggeun Lee, Tanya M Teslovich, Michael Boehnke, et al.Biorxiv : the Preprint Server for Biology|December 25, 2025
Trajectory-informed gene feature selection in single-cell analysis with SEEK-VFIRebecca Danning, Zheng Tracy Ke, Xihong Lin, et al.Pageof 45